Test Price
2,800 AED✅ Home Collection Available
HIBCH Gene 3‑Hydroxyisobutyryl‑CoA Hydrolase Deficiency Genetic Test in UAE | 2800 AED
Executive Summary & Core Metrics
Diagnostic Precision 99.9% Diagnostic Sensitivity – ISO 9001:2015 Accredited Processing
Premium Home Collection: Hospital‑grade, cold‑chain sample transport; VIP mobile phlebotomy available 8 AM–11 PM daily.
Clinical Guidance: Telephonic post‑test interpretation by certified genetic counsellors.
Insurance Support: Direct billing verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
The HIBCH Gene NGS Test detects pathogenic variants in the 3‑hydroxyisobutyryl‑CoA hydrolase gene, confirming the diagnosis of a rare inborn error of valine metabolism. Performed on peripheral blood samples using Next‑Generation Sequencing (NGS) with full gene coverage, results are delivered in 3–4 weeks. The test includes mandatory pre‑ and post‑test genetic counselling.
| Feature | Our Test (ISO/DHA) | Closest Alternative |
|---|---|---|
| Methodology | Next‑Generation Sequencing (NGS) – full gene coverage | Sanger sequencing (single exon) |
| Turnaround Time | 3–4 weeks | 6–8 weeks |
| Sample Types | Blood, Extracted DNA, FTA Card | Blood only |
| Genetic Counselling | Mandatory pre‑test session included | Not offered |
| Insurance Billing | Direct verification via WhatsApp | Self‑pay only |
Physician Insight & Safety Protocols
“As a clinical geneticist, I emphasise that a positive HIBCH result must always be correlated with clinical findings and metabolic investigations. This test is a powerful diagnostic tool, but it is only one piece of the puzzle. Every result is reviewed by our multidisciplinary team to provide a comprehensive interpretation.”
– Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA Registration ID: 9294403
Advisory Precautions
Important Medication Advisory
Do not discontinue or alter any prescribed medications without consulting your treating physician. This genetic test does not replace therapeutic management.
Safety Exclusion Criteria & Red Flags
- Exclusion: Acute febrile illness or haemodynamic instability on the day of sample collection.
- Exclusion: Inability to provide informed consent or assent; for minors, legal guardian consent is mandatory as per Federal Decree-Law No. 4 of 2016 on Medical Liability.
- Red Flag: Sudden neurological deterioration, intractable vomiting, or seizures in a child undergoing testing – seek emergency care immediately.
Patient FAQ & Clinical Guidance
1. Who should consider the HIBCH gene test?
This test is indicated for infants and children presenting with developmental regression, hypotonia, and metabolic acidosis suggestive of a valine metabolism defect. It is also offered to at‑risk family members after genetic counselling. The test must be ordered by a qualified physician.
2. How is the sample collected for this DNA test?
A certified phlebotomist draws a small blood sample or collects a buccal swab at your home in Dubai and Abu Dhabi. FTA cards are also accepted for remote locations. The sample is transported under cold‑chain protocols. Our mobile phlebotomy service is available daily from 8 AM to 11 PM.
3. Is genetic counselling mandatory before testing?
Yes, a mandatory pre‑test genetic counselling session with a certified genetic counsellor is included in the service. The counsellor reviews your family history, draws a pedigree chart, and explains potential outcomes. Post‑test counselling is also provided to discuss results.
UAE Regulatory & Data Privacy Adherence
✓ ISO 9001:2015 Certified – Cert: INT/EGQ/2509DA/3139 | DHA Facility License: 1143
Data privacy governed by Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL) and Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields. All genetic data is encrypted and stored in UAE-local servers.
Clinical & Logistical Metadata
| Test Name | HIBCH Gene 3‑Hydroxyisobutyryl‑CoA Hydrolase Deficiency Genetic Test |
| Price (AED) | 2,800 AED |
| Turnaround Time | 3–4 weeks |
| Sample Type / Matrix | Peripheral whole blood, extracted DNA, FTA card (buccal swab accepted) |
| Methodology Used | Next‑Generation Sequencing (NGS) – full gene coverage |
| ICD-10-CM Code | E71.19 |
| LOINC Code | 82939-0 |
| DHA Facility License & Laboratory Address | DHA License: 1143 | Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE – DNA Labs UAE |
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ISMS 27001:2022
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All reports reviewed by DHA-Certified physicians